05/04/2024 | Fulltime | | Germany | CV-Library | €70,000 - €80,000 / Year With ISO related to med-tech such as 13485, ISO 14971 (or ISO 9001) and FDA - Experience with regulatory affairs for medical devices and QMS - Knowledge of, or experience with, in-vitro diagnostic medical devices regulation (MDD - MDR) IVDR and CFR - Exceptional communication skills, attention to detail
Save for later